Variant #0000178786 (NC_000004.11:g.73179445C>T, NM_014243.2:c.1694G>A (ADAMTS3))

Chromosome 4
Allele Paternal (inferred)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.73179445C>T
DNA change (hg38) g.72313728C>T
Published as R565Q
ISCN -
DB-ID ADAMTS3_000003 See all 3 reported entries
Variant remarks -
Reference PubMed: Jha et al., 2017
ClinVar ID -
dbSNP ID rs141374503
Origin Germline
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00215 View details
Owner Pascal Brouillard
Database submission license No license selected
Created by Pascal Brouillard
Date created 2017-08-01 10:25:04 +02:00 (CEST)
Date last edited 2020-03-29 12:37:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADAMTS3 NM_014243.2 +/+ 12 c.1694G>A r.(?) p.(Arg565Gln)


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